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dc.contributor.authorGeorge K.K. Lauen_US
dc.contributor.authorTeerha Piratvisuthen_US
dc.contributor.authorXian Luo Kangen_US
dc.contributor.authorPatrick Marcellinen_US
dc.contributor.authorSatawat Thongsawaten_US
dc.contributor.authorGraham Cooksleyen_US
dc.contributor.authorEdward Ganeen_US
dc.contributor.authorMichael W. Frieden_US
dc.contributor.authorCheng Chow Wanen_US
dc.contributor.authorWoon Paik Seungen_US
dc.contributor.authorYu Chang Wenen_US
dc.contributor.authorThomas Bergen_US
dc.contributor.authorRobert Flisiaken_US
dc.contributor.authorPhilip McClouden_US
dc.contributor.authorNigel Plucken_US
dc.date.accessioned2018-09-11T09:26:29Z-
dc.date.available2018-09-11T09:26:29Z-
dc.date.issued2005-06-30en_US
dc.identifier.issn15334406en_US
dc.identifier.issn00284793en_US
dc.identifier.other2-s2.0-21244447705en_US
dc.identifier.other10.1056/NEJMoa043470en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=21244447705&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/62382-
dc.description.abstractBACKGROUND: Current treatments for chronic hepatitis B are suboptimal. In the search for improved therapies, we compared the efficacy and safety of pegylated interferon alfa plus lamivudine, pegylated interferon alfa without lamivudine, and lamivudine alone for the treatment of hepatitis B e antigen (HBeAg)-positive chronic hepatitis B. METHODS: A total of 814 patients with HBeAg-positive chronic hepatitis B received either peginterferon alfa-2a (180 μg once weekly) plus oral placebo, peginterferon alfa-2a plus lamivudine (100 mg daily), or lamivudine alone. The majority of patients in the study were Asian (87 percent). Most patients were infected with hepatitis B virus (HBV) genotype B or C. Patients were treated for 48 weeks and followed for an additional 24 weeks. RESULTS: After 24 weeks of follow-up, significantly more patients who received peginterferon alfa-2a monotherapy or peginterferon alfa-2a plus lamivudine than those who received lamivudine monotherapy had HBeAg seroconversion (32 percent vs. 19 percent [P<0.001] and 27 percent vs. 19 percent [P=0.02], respectively) or HBV DNA levels below 100,000 copies per milliliter (32 percent vs. 22 percent [P=0.01] and 34 percent vs. 22 percent [P=0.003], respectively). Sixteen patients receiving peginterferon alfa-2a (alone or in combination) had hepatitis B surface antigen (HBsAg) seroconversion, as compared with 0 in the group receiving lamivudine alone (P=0.001). The most common adverse events were those known to occur with therapies based on interferon alfa. Serious adverse events occurred in 4 percent, 6 percent, and 2 percent of patients receiving peginterferon alfa-2a monotherapy, combination therapy, and lamivudine monotherapy, respectively. Two patients receiving lamivudine monotherapy had irreversible liver failure after the cessation of treatment - one underwent liver transplantation, and the other died. CONCLUSIONS: In patients with HBeAg-positive chronic hepatitis B, peginterferon alfa-2a offers superior efficacy over lamivudine, on the basis of HBeAg seroconversion, HBV DNA suppression, and HBsAg seroconversion. Copyright © 2005 Massachusetts Medical Society. All rights reserved.en_US
dc.subjectMedicineen_US
dc.titlePeginterferon Alfa-2a, lamivudine, and the combination for HBeAg-positive chronic hepatitis Ben_US
dc.typeJournalen_US
article.title.sourcetitleNew England Journal of Medicineen_US
article.volume352en_US
article.stream.affiliationsThe University of Hong Kongen_US
article.stream.affiliationsSongklanakarin Hospitalen_US
article.stream.affiliationsNanfang Hospitalen_US
article.stream.affiliationsHopital Beaujonen_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsRoyal Brisbane Hospitalen_US
article.stream.affiliationsMiddlemore Hospital, Aucklanden_US
article.stream.affiliationsThe University of North Carolina at Chapel Hillen_US
article.stream.affiliationsSingapore General Hospitalen_US
article.stream.affiliationsSungKyunKwan University, School of Medicineen_US
article.stream.affiliationsKaohsiung Medical University Chung-Ho Memorial Hospitalen_US
article.stream.affiliationsCharité – Universitätsmedizin Berlinen_US
article.stream.affiliationsUniwersytet Medyczny w Bialymstokuen_US
article.stream.affiliationsRocheen_US
article.stream.affiliationsRoche Products Limited UKen_US
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